1. The length of the Y-chromosomes in men examined by forensic psychiatrists

   • Hans Olof Åkesson
   • Jan Wahlström

   Original Investigations Pages: 1 - 5

2. Risk for short arm 10 trisomy

   • J. Stene
   • S. Stengel-Rutkowski

   Original Investigations Pages: 7 - 13

3. Split hand and foot deformity and the syndrome of ectrodactyly, ectodermal dysplasia, and clefting (EEC)

   • Rina Schmidt
   • Harold M. Nitowsky

   Original Investigations Pages: 15 - 25

4. Meiosis I non-disjunction as the main cause of trisomy 21

   • Jacqueline A. Robinson

   Original Investigations Pages: 27 - 30

5. LBA technique in the detection of chromosome variants

   • S. Oka
   • Y. Nakagome
   • M. Arima

   Original Investigations Pages: 31 - 37

6. Distribution of human chromosomes on the metaphase plate using banding techniques

   • B. Sele
   • P. Jalbert
   • R. Bouchez

   Original Investigations Pages: 39 - 61

7. Alpha-1-Antitrypsin phenotypes in Lyon, France

   • Phillippe Arnaud
   • C. Chapuis-Cellier
   • R. Creyssel

   Original Investigations Pages: 63 - 68

8. Absence of a relationship between degree of white ancestry and intellectual skills within a black population

   • Sandra Scarr
   • Andrew J. Pakstis
   • William B. Barker

   Original Investigations Pages: 69 - 86

9. Cell division and sister chromatid exchanges in 45,X/46,X,i(Xq) mosaicism

   • Kyra Michalová
   • Jana Málková
   • Josef Urban

   Short Communications Pages: 87 - 90

10. Polymorphism of red cell glyoxalase 1

    • A. K. Ghosh

    Short Communications Pages: 91 - 95

11. Syndrome +12p

    • Romano Tenconi
    • Emanuela Piovan
    • Carlo Baccichetti

    Clinical Case Reports Pages: 97 - 101

12. Down and Turner syndromes in a female infant with 47,X,del(X)(p11),+21

    • John T. Martsolf
    • M. Ray
    • J. D. Armstrong

    Clinical Case Reports Pages: 103 - 108

13. Cri-du-chat Syndrome in a child with a 46,XX,der(5),t(4;5)(q32;p14)pat karyotype

    • Alan McDermott
    • Ray Poulding
    • Desmond Creery

    Clinical Case Reports Pages: 109 - 112

14. Lymphedema — Distichiasis

    • Hans Georg Jester

    Clinical Case Reports Pages: 113 - 116

15. Yq deletion, aspermia, and short stature

    • Emilio Yunis
    • Francisco L. García-Conti
    • Alejandro Giraldo

    Clinical Case Reports Pages: 117 - 122

16. Studies of the meiotic behavior of a translocation t(10;13)(q25;q11) in an oligospermic man

    • C. Laurent
    • M. -Cl. Biemont
    • B. Dutrillaux

    Clinical Case Reports Pages: 123 - 126

17. Unusual translocation (10;22) in chronic myelogenous leukemia

    • E. W. Fleischman
    • E. L. Prigogina
    • I. Petkovitch

    Clinical Case Reports Pages: 127 - 129

18. A new case of XX-male (XX/XXY mosaic)

    • P. Kaiser
    • K. Gerhard-Ratschow
    • W. Gey

    Clinical Case Reports Pages: 131 - 137

19. A sibship with hypervalinemia

    • O. S. Reddi
    • S. V. Reddy
    • K. R. S. Reddy

    Clinical Case Reports Pages: 139 - 142

20. Familial incidence of L-Xylulosuria

    • O. S. Reddi
    • S. V. Reddy
    • K. R. Reddy

    Clinical Case Reports Pages: 143 - 145